Rapid exchange catheters and embolic protection devices

ABSTRACT

A catheter compiling a housing portion defining an interior cavity and the housing portion comprising a housing member having an interior space dimensioned for housing an indwelling medical device. The elongated member comprises a lumen extending at least from an exit port to a distal port, the housing member is disposed within the lumen, and the lumen is dimensioned in the housing portion to receive a guidewire outside of the interior space of the housing member. A medical device for filtering emboli from blood flowing in a blood vessel of patient comprising an elongate support member and an elongate side branch member connected to the elongate support member. The filter element is attached to the elongate side branch member by a proximal filter element slider, and the elongate side branch member is adapted to maintain the filter element centered in the vessel.

This application is a continuation of U.S. application Ser. No.13/149,464, filed May 31, 2011, now U.S. Pat. No. 9,456,889, which is acontinuation of U.S. application Ser. No. 11/357,404, filed Feb. 17,2006, now U.S. Pat. No. 7,955,351, which claims the benefit of U.S.Provisional Application No. 60/654,389, filed Feb. 18, 2005, thecontents of each of which are hereby incorporated by reference herein.

FIELD OF THE INVENTION

This invention relates to devices used in a blood vessel or other lumenin a patient's body, in particular, the present invention relates torapid exchange catheters and embolic protection devices that may bedelivered thereby.

BACKGROUND OF THE INVENTION

Coronary vessels, partially occluded by plaque, may become totallyoccluded by thrombus or blood clot causing myocardial infarction,angina, and other conditions. Carotid, renal, peripheral, and otherblood vessels can also be restrictive, to blood flow and requiretreatment. A number of medical procedures have been developed to allowfor the removal or displacement (dilation) of plaque or thrombus fromvessel walls to open a channel to restore blood flow and minimize therisk of myocardial infarction. For example, atherectomy or thrombectomydevices can be used to remove atheroma or thrombus. In cases whereinfusion of drugs or aspiration of thrombus may be desired, infusion oraspiration catheters can be placed near the treatment site to infuse oraspirate. In cases where the treatment device can be reasonably expectedto shed emboli, embolic protection devices can be placed near thetreatment site to capture and remove emboli. In other cases, a stent isplaced at the treatment site. Both embolic protection devices and stentscan be placed in or near the treatment site using delivery catheters.

In percutaneous transluminal coronary angioplasty (PICA), a guidewireguide catheter are inserted into the femoral artery of a patient nearthe groin, advanced through the artery, over the aortic arch, and into acoronary artery. An inflatable balloon is then advanced into thecoronary artery, across a stenosis or blockage, and the balloon inflatedto dilate the blockage and open a flow channel through the partiallyblocked vessel region. One or more stents may also be placed across thedilated region or regions to structurally maintain the open vessel.Balloon expandable stents are crimped onto a balloon in the deflatedstate and delivered to the lesion site. Balloon expansion expands thestem against the lesion and arterial wall. Alternatively, self-expandingstents can be restrained in a sheath, delivered to the treatment site,and the sheath removed to allow expansion of the stem.

Embolic protection devices have been developed to prevent the downstreamtravel of materials such as thrombi, grunions, emboli, and plaquefragments. Devices include occlusive devices and filters. Occlusivedevices, for example distal inflatable balloon devices, can totallyblock fluid flow through the vessel. The material trapped by theinflatable devices can remain in place until removal using a method suchas aspiration. However, aspiration cannot remove large particles becausethey will not fit through the aspiration lumen. Also, aspiration is aweak acting force and will not remove a particle unless the tip of theaspirating catheter is very close to the particle to be removed. Duringthe occlusion, the lack of fluid flow can be deleterious. In coronaryapplications, the lack of perfusing blood flow can cause angina. Incarotids, seizure can result from transient blockage of blood flow, inboth coronaries and carotids, it is not possible to predict who willsuffer from angina or seizure due to vessel occlusion. If a procedurestarts with an occlusive device, it may be necessary to remove it andstart over with a filter device.

Occlusive embolic protection devices can also be placed proximal to thetreatment site. Debris generated at or near the treatment site will notbe transported from the treatment site if a proximal occlusive devicesubstantially stops blood flow through the vessel. The materialgenerated during treatment can remain in place until removal using amethod such as aspiration. Generally, proximal occlusive embolicprotection devices suffer from many of the same limitations as distalocclusive embolic protection devices.

Other catholic protection devices are filters. Filters can allowperfusing blood flow during the emboli capture process. The filters canadvance downstream of a site to be treated and expand to increase thefilter area. The filter can capture emboli, such as grumous or atheromafragments, until the procedure is complete or the filter is occluded.When the filter reaches its capacity, the filter may then be retractedand replaced.

Embolic protection devices can be delivered over wires and within guidecatheters. The embolic protection methods are normally practicedancillary to another medical procedure, for example PTCA with stentingor atherectomy. The embolic protection procedure typically protectsdownstream regions from emboli resulting from practicing the therapeuticinterventional procedure. In the example of PTCA, the treating physicianmust advance a guidewire through the aorta, over the aortic arch, andinto a coronary ostium. Advancing the guidewire through tortuous vesselsfrom a femoral artery approach can be difficult and vary with both thepatient and the vessel site to be treated. Guide wires are typicallyselected by the treating physician, based on facts specific to thepatient and therapeutic situation, and also on the training, experience,and preferences of the physician. In particular, a physician may havebecome very efficient in using a specific guidewire to access the leftcoronary ostium and then advance a balloon catheter over the positionedguidewire. The efficacy of the procedure may depend on the physicianbeing able to use a favored guidewire.

In the example PTCA procedure, a guide catheter extends proximally fromthe patient's groin area, and may be about 100 centimeters long. A 320centimeter guidewire is placed into the guide catheter and extendeddistal of the guide into a coronary vessel, leaving about a 200centimeter long guidewire proximal region extending from the guidecatheter. The embolic protection device delivery catheter, nominallyabout 130 centimeters in length, can advance over the guidewire andwithin the guide catheter, until a length of guidewire extends from boththe guide catheter and delivery catheter. The guidewire can then beretracted and removed from the patient. In some methods, the embolicprotection device then advances through and out of the positioneddelivery catheter, to the target site to be protected or filtered. Inother methods, delivery is accomplished by disposing the embolicprotection filter device within the delivery catheter distal region, andadvancing the delivery catheter and embolic protection device togetherwithin the guide catheter, optionally over the guidewire, and deployingthe filter by retracting the delivery catheter while maintaining theposition of the filter, thus forcing the filter distally out of thedelivery catheter.

Advancement of the delivery catheter over a single length, nominally 170centimeter long guidewire presents a problem. The treating physician canonly advance the filter delivery catheter about 40 centimeters over theguidewire until the delivery catheter advances into the patient and theguidewire is inaccessible within the delivery catheter. The guidewireposition should be controlled at all times so as to not be dislodged bythe advancing delivery catheter from the hard acquired guidewireposition within the patient.

One solution to this problem is to use a guidewire at least double thelength of the delivery catheter as described above. A 320 centimeterlong guidewire can extend at least about 150 centimeters from thepatient's groin, having an accessible region exposed at all phases ofdelivery catheter placement. However, the length of the 320 centimeterguidewire makes manipulating and rotating the guidewire very difficultfor the treating physician, Additional personnel can hold the extralength of the guidewire to prevent the added wire length front fallingto the floor, where it would become contaminated. However, not allcardiac catheter laboratories have personnel available to maintaincontrol of the long guidewire. In many labs, the physician is workingalone in the sterile field. Advancing a device delivery catheter over apositioned, favored, and short (175 centimeter) guidewire would beinherently more efficacious than requiring use of an unfamiliar,disfavored, or double length guidewire to position the deliverycatheter.

Another alternative catheter design is the monorail or rapid exchangetype such as that disclosed in U.S. Pat. No. 4,762,129, issued Aug. 9,1988, to Bonzel. This catheter design utilizes a conventional inflationlumen plus a relatively short parallel guiding or through lumen locatedat its distal end and passing through the dilatation balloon. Guidewires used with PTCA balloon catheters are typically 175 centimeters inlength and are much easier to keep within the sterile operating fieldthan 300 to 340 centimeter guidewires. This design enables the shortexternally accessible rapid exchange guidewire lumen to be threaded overthe proximal end of a pre-positioned guidewire without the need for longguidewires.

Still needed in the art are improved designs for rapid exchange deliverycatheters. Such delivery catheters can be used to deliver varioustreatment and/or diagnostic devices including embolic protectiondevices.

It is desirable to place a distal protection device at a chosen locationin order to achieve good seating between the device and the wall of thevessel. Frequently it is necessary to match the protection devicediameter with the vessel diameter, and vessels are known to taper or tohave diameters that vary due to disease. It is also desirable to placethe protection device in a relatively disease free portion of the vesselso as to minimize liberation of emboli from the wall of the vessel dueto interaction with the protection device. Further, it is desirable thatthe device remains at the desired location during the procedure.Excessive motion of the wire or elongate guide member used to deliverthe device can advance a protection device distally, beyond branchvessels, which thereby become unprotected from emboli.

Distal protection devices typically are mounted on a wire or tube thatfunctions as a guidewire. As used herein the term guidewire means eithera traditional guidewire or other elongate member or hollow tube that isused in delivering the distal protection device. The protection devicecan be either a filter or an occlusive device such as a balloon. Thedistal protection devices are either fixedly attached to the guidewireor attached so as to permit a limited amount of motion between thedevice and the guidewire. Frequently, the same guidewire used to carrythe devices used to guide various catheters to and from the treatmentsite. For example, during the procedure, catheters may be exchanged overthis guidewire. When catheters are exchanged inadvertent wire movementcan cause the protection device to move within the vessel. Excessivewire motion can also retract a protection device proximally, where itcan potentially become entangled in a stem or even be inadvertentlyremoved from the vessel being protected. In some vessels, when guidecatheters are repositioned, the protection device also tends to movewithin the vessel. This is undesirable because captured emboli can bereleased and/or new emboli can be formed distal to the protectiondevice, blood vessels can be damaged, and/or the device can entanglewith an implant such as a stent. Therefore, it is clear that too muchmovement of the device within the vessel could have catastrophicresults.

Some work already has been done to provide for limiting the movement ofa distal protection device or distal filer with respect to a guidewire.For example, a guidewire having a distal stop is described in WO01/35857 (Tsugita et al.). The filter slides on the guidewire hut cannotslide off the wire due to the distal stop. Another device which includesa slideable vascular filter having both distal and proximal slidingelements that move independently of each other over a mandrel isdescribed in WO 01/21100 (Kusleika et al). While this system meets manyof the needs in the art, it limits the range of motion of the filtrationdevice on the guidewire, and the precision with which it can be placedis limited. Still further embodiments of devices which allow increasedindependence of movement of the guidewire without moving the embolicprotection device are disclosed in U.S. Pat. No. 6,773,448 B2, issuedAug. 10, 2004, to Kusleika et al.

Another known limitation of distal protection devices relates to winbias. It is well known that a guidewire will conform to the outsidevessel on advancement of the wire in a distal direction and will conformto the interior of a curved vessel during retraction of the wire. Mostdistal protection devices are attached to wires, and when they aredeployed in vessel curvature the wire bias will alternately move thedevice between the inside and the outside of the vessel curve. Forfilters this can defeat the protection effect by compressing the filteropening. For occlusion devices the wire bias effect can cause excessivemotion of the occlusion device with potential liberation of embolicdebris from the vicinity of the occlusive element.

Some work already has been done to provide for limiting the radialmovement of a guidewire relative to a distal protection device. Forexample, a protection device having a proximal loop is described in U.S.Pat. No. 6,740,061 B1, issued May 25, 2004, to Oslund et al.), thecontents of which are incorporated herein by reference. A loop isprovided proximal to the filter to immobilize the wire against thevessel wall regardless of wire bias. While this system meets many of theneeds in the art, it adds bulk to the device and thereby limits crossingprofile.

It would be desirable to have a distal protection system that can beprecisely placed at a location within the vasculature and that canaccommodate some range of axial and/or radial wire motion withoutdisturbing the device's position. Further, when the embolic protectiondevice is a filter it would be desirable that the host wire whichcarries the filter be centered within the lumen when the device isdeployed.

SUMMARY OF THE INVENTION

The present invention provides a rapid exchange catheter which can beused to deliver various vascular treatment and/or diagnostic devices.The invention also provides an improved embolic protection device whichcan be delivered, for example, by the rapid exchange catheter disclosedherein.

The invention provides a catheter comprising: an elongated memberconfigured to be advanced along a vascular path of a patient, theelongated member having a proximal portion, a distal portion, a proximalend, a distal end, a housing portion adjacent to and proximal of thedistal portion, and a sidewall exit port proximal of the housingsection; the distal end comprising a distal port; the distal portioncomprising an indwelling medical device delivery structure; the housingportion defining an interior cavity and the housing portion comprising ahousing member having an interior space dimensioned for housing anindwelling medical device; the elongated member comprising a lumenextending at least from the exit port to the distal port, the housingmember being disposed within the lumen, and the lumen being dimensionedin the housing portion to receive a guidewire outside of the interiorspace of the housing member.

The invention further provides a method for positioning a medical devicewithin a patient's blood vessel, the method comprising: providing acatheter described herein and advancing the medical device to a targetsite within the patient's blood vessel.

The invention provides a method for positioning a catheter within apatient's blood vessel, the method comprising: providing a catheterdescribed herein; providing a guidewire having a proximal end and adistal end; advancing the guidewire to a larger site within thepatient's blood vessel; and advancing the catheter over the guide wireby inserting the guidewire through the lumen between the distal port andthe sidewall exit port.

The invention further provides a distal tip of a host wire of an embolicprotection device comprising: a wire comprising a first constantdiameter region having a first diameter, a second constant diameterregion baying a second diameter, and a third constant diameter regionhaving a third diameter, the second constant diameter region having asmaller diameter than the first constant diameter region, and the thirdconstant diameter region having a smaller diameter than the secondconstant diameter region; a first tapering transition region between thefirst constant diameter region and the second constant diameter region;and a second tapering transition region between the second constantdiameter region and the third constant diameter region.

The invention provides a medical device for maintaining an embolicprotection device in a blood vessel in a patient's body comprising: anelongate support member, an elongate side branch member connected to theelongate support member; and an embolic protection device attached tothe elongate side branch member by a proximal embolic protection deviceslider, the elongate side branch member being adapted to maintain theembolic protection, device centered in the vessel.

The invention further provides a medical device for filtering embolifrom blood flowing in a blood vessel of patient comprising: an elongatesupport member; an elongate side branch member connected to the elongatesupport member; and a filter element being expandable from a collapsedconfiguration when the filter element is restrained to an expandedconfiguration when the filter element is unrestrained, wherein thefilter element comprises a material having pores, wherein the filterelement has proximal and distal portions, the filter element having ashape in the expanded configuration which defines an interior cavityhaving a proximal facing opening, the filter element being attached tothe elongate side branch member by a proximal filter element slider, theelongate side branch member being adapted to maintain the filter elementcentered in the vessel.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a double-ended catheter having features that are examplesof inventive aspects in accordance with the principles of the presentdisclosure.

FIG. 2 is a schematic view of a portion of the delivery end of thedouble-ended catheter of FIG. 1.

FIGS. 3A and 38 are cross-sectional views of a portion of the deliveryend of the catheter of FIG. 1 according to a first embodiment of theinvention.

FIG. 4 is a perspective view of a stop member shown in FIGS. 3A and 3B.

FIGS. 5A, 5B and 5C are cross-sectional views of a portion of thedelivery end of the catheter of FIG. 1 according to further embodimentsof the invention.

FIGS. 6A and 6B are alternate embodiments of a housing member shown inFIG. 5A.

FIGS. 7A and 7B are views of a grommet utilized in the embodiments ofFIGS. 5C and 5B respectively.

FIGS. 8A to 8F disclose steps in the method of loading and using adelivery catheter in accordance with be present invention.

FIGS. 9A and 9B disclose features of the distal tip of a support wireand delivery catheter, respectively, in accordance with the presentinvention.

FIGS. 10A and 10B disclose use of a removable packaging sheath to flushthe catheter of the present invention prior to use.

FIG. 11 shows an embolic protection device.

FIGS. 12 to 17 show various embodiments of an embolic filtration devicein accordance with the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The terms “distal” and “proximal” as used herein refer to the relativeposition of the guidewire and catheters in a lumen. The most “proximal”point of the catheter is the end of the catheter extending outside thebody closest to the physician. The most “distal” point of the catheteris the end of the catheter placed farthest into a body lumen from theentrance site. The same meaning is applied to these terms when used indescribing an embolic protection device.

The use of the phrases “distal embolic protection device” or “embolicprotection device” herein refers to embolic protection devices that areocclusive, diverting, and/or filtering. The term “embolic protectiondevice” is meant to include devices used to protect a target site andlocated either proximal to, at, or distal to the treatment site.

The invention provides a catheter comprising an elongated memberconfigured to be advanced along a vascular path of a patient, theelongated member having a proximal portion, a distal portion, a proximalend, a distal end, a housing portion adjacent to and proximal of thedistal portion, and a sidewall exit port proximal of the housingsection; the distal end comprising a distal port; the distal portioncomprising an indwelling medical device delivery structure; the housingportion defining an interior cavity and the housing portion comprising ahousing member having an interior space dimensioned for housing anindwelling medical device; the elongated member comprising a lumenextending at least from the exit port to the distal port, the housingmember being disposed within the lumen, and the lumen being dimensionedin the housing portion to receive a guidewire outside of the interiorspace of the housing member. In one embodiment, the housing member issecured at a fixed location within the housing portion. In anotherembodiment, the housing portion comprises distal and proximal housingsections and the housing member can move axially within the housingportion. In another embodiment, the housing member can move axiallybetween the proximal and distal sections of the housing portion.

In one embodiment, the housing portion and distal portion have outerdiameters and the outer diameter of the housing portion is larger thanthe outer diameter of the distal portion. In another embodiment, thehousing portion and distal portion have inner diameters and the innerdiameter of the housing portion is larger than the inner diameter of thedistal portion. In another embodiment, the housing portion and distalportion have outer diameters and the outer diameter of the housingportion is larger than the outer diameter of the distal portion, and thehousing portion and distal portion have inner diameters and the innerdiameter of the housing portion is larger than the inner diameter of thedistal portion.

In one embodiment, the proximal housing section comprises a stop member.The stop member may be tubular. The stop member may comprise one or moresidewall slots that allow additional pathways for the guidewire.

In one embodiment, the elongated member has an inner wall defining thelumen and the housing member is adjacent to the inner wall. In anotherembodiment, the housing member is centered within the lumen.

In one embodiment, the housing, portion comprises distal and proximalhousing sections and the proximal housing section comprises the housingcomprise one or more sidewall slots that allow additional pathways for aguidewire.

In one embodiment, wherein the elongated member has an inner walldefining the lumen, and the housing member is suspended within thehousing portion by a grommet that is affixed to the inner wall. In anembodiment, the grommet has an outer periphery, and the entire outerperiphery of the grommet contacts the inner wall. The housing member maybe centered within the lumen. The grommet may comprise one OT moreopenings which allow passage of the guidewire. In one embodiment, thegrommet comprises a single opening that allows passage of the guidewire,and in another embodiment the grommet comprises two openings that allowpassage of the guidewire.

The housing member may be tabular. The catheter may comprise a ramp inthe lumen that causes a guidewire to be directed out the exit port. Inone embodiment, at least a portion of the housing portion istransparent.

The proximal portion of the catheter may comprise an indwelling medicaldevice retrieval structure. The proximal portion may comprise a sidewallport. The proximal end of the catheter may comprise a rolled tip. Theproximal end of the catheter may comprise a shapeable tip.

In one embodiment, the distal port has a diameter and the distal endcomprises a removable delivery tip transition component that reduces thediameter of the distal port. The removable delivery tip transitioncomponent may comprise a tearable spirally wrapped material and a stringthat extends along the side of the delivery catheter.

The invention provides an assembly comprising a guidewire and a catheterdescribed herein. The invention provides an assembly comprising amedical device and a catheter described herein. The assembly may furthercomprise a guidewire. The medical device can be selected from an embolicprotection device, balloon catheter, stent delivery catheter, atrialappendage occlusion device, mitral valve remodeling device, or septaldefect closure device. In one embodiment, the medical device is anembolic protection device. In one embodiment the embolic protectiondevice is a filter, and in another embodiment, embolic protection deviceis an occlusive device. In one embodiment, the medical device is adaptedto be delivered and retrieved by the elongated member.

The invention provides an assembly comprising a catheter describedherein and a removable packaging sheath having an end adapted toaccommodate a fluid filled syringe for flushing the catheter.

The invention provides a method for positioning a medical device withina patient's blood vessel, the method comprising: providing a catheterdescribed herein; and advancing the medical device to a target sitewithin the patient's blood vessel.

The invention provides a method for positioning a catheter within apatient's blood vessel, the method comprising: providing a catheterdescribed herein; providing a guidewire having a proximal end and adistal end; advancing the guidewire to a target site within thepatient's blond vessel; and advancing the catheter over the guide wireby inserting the guidewire through the lumen between the distal port andthe sidewall exit port. In one embodiment, the embolic protection deviceis leaded into the catheter prior to advancing the catheter over theguide wire. In an embodiment, the catheter is advanced over the guidewire to a treatment site, the guide wire is removed, and the embolicprotection device is advanced out of the catheter.

The invention provides a distal tip of a host wire of an embolicprotection device comprising: a wire comprising a first constantdiameter region having a first diameter, a second constant diameterregion having a second diameter, and a third constant diameter regionhaving a third diameter, the second constant diameter region having asmaller diameter than the first constant diameter region, and the thirdconstant diameter region having a smaller diameter than the secondconstant diameter region; a first tapering transition region between thefirst constant diameter region and the second constant diameter region;and a second tapering transition region between the second constantdiameter region and the third constant diameter region.

The invention provides a medical device for maintaining an embolicprotection device in a blood vessel in a patient's body comprising: anelongate support member; an elongate side branch member connected to theelongate support member; and an embolic protection device attached tothe elongate side branch member by a proximal embolic protection deviceslider, the elongate side branch member being adapted to maintain theembolic protection device centered in the vessel. In one embodiment, theelongate side branch member is adapted to maintain the elongate supportmember centered in the lumen. In another embodiment, the embolicprotection device is attached to the elongate support member. Theembolic protection device may be a filter or an occlusive device.

The invention provides a medical device for filtering emboli from bloodflowing in a blood vessel of patient comprising: an elongate supportmember; an gate side branch member connected to the elongate supportmember; and a filter element being expandable from a collapsedconfiguration when the filter element is restrained to an expandedconfiguration when the filter element is unrestrained, wherein thefilter element comprises a material having pores, wherein the fillerelement has proximal and distal portions, the filter element having ashape in the expanded configuration which defines an interior cavityhaving a proximal facing opening, the filter element being attached tothe elongate side branch member by a proximal filter element slider, theclot side branch member being adapted to maintain the filter elementcentered in the vessel. In one embodiment, the elongate side branchmember is adapted to maintain the elongate support member centered inthe lumen. In another embodiment, the material having pores isself-expanding. In another embodiment, the material having porescomprises wires braided to form pores.

In one embodiment, the elongate support member has distal and proximalportions and the filter element is attached, to the elongate supportmember in a distal portion of the elongate support member. In anotherembodiment, the elongate support member has a distal end and the filterelement attached to the elongate support member at or near the distalend.

In one embodiment, the elongate side branch member is connected to theelongate support member by a proximal side branch member slider and adistal side branch member slider. In another embodiment, the filterelement is attached to the elongate support member by a distal filterelement slider. In one embodiment, when the medical device is in itsexpanded configuration, (i) the proximal side branch member slider isproximal of the proximal filter element slider, (ii) the proximal filterelement slider is proximal of the distal side branch member slider, and(iii) the distal side branch member slider is proximal of the distalfilter element slider. In one embodiment, the elongate support memberincludes a proximal stop and a distal stop with both stops being distalto the distal side branch member slider and proximal of the distalfilter element slider.

In one embodiment, the elongate side branch member is connected to theelongate support member by a proximal side branch member slider. In anembodiment, the elongate side branch member has a distal end thatcomprises a distal end stop and the distal end is not connected to theelongate support member. In one embodiment, the fitter element isattached to the elongate support member by a distal filter elementslider. In an embodiment, when the medical device is in its expandedconfiguration, the proximal side branch member slider is proximal of theproximal filter element slider. In one embodiment, the elongate memberincludes an elongate member stop, the elongate member stop being distalof the proximal side branch member slider and being proximal of thedistal filter element slider.

In one embodiment, the elongate support member has a distal end portionand the elongate side branch member is a loop portion of the elongatesupport member at the distal end portion. In an embodiment, the proximalfilter element slider provides the only connection between the filterelement and the elongate side branch member, and the filter element isnot connected to the elongate support member.

In one embodiment, the filter element is attached to the elongate sidebranch member by the proximal filter element slider and a distal filterelement slider. In an embodiment, the elongate support member has adistal end, a tube is fixed on the elongate side branch member betweenthe proximal and distal filter element sliders, and the tube slideablyreceives the distal end of the elongate support member.

In one embodiment, the elongate support member comprises a slot in whicha sliding element is disposed and the elongate side branch member isconnected to the elongate support member by the proximal slidingelement. In an embodiment, a distal dual side branch member and filterelement slider connects the elongate side branch member and the filterelement to the elongate support member.

In one embodiment be elongate side branch member is connected to theelongate support member by a proximal side branch member slider and adistal dual side branch member and filter element slider, the distaldual side branch member and filter element slider connecting the filterelement to the elongate support member. In an embodiment, the elongatemember includes a stop distal to the proximal side branch member sliderand proximal of the distal dual side branch member and filter elementslider.

A. Rapid Exchange Delivery Catheter

In the drawing figures included herein the rapid exchange deliverycatheter is shown as comprising one end of a double ended catheter. Theother end of the catheter is used for recovering a medical device from alumen. A similar catheter is disclosed in U.S. Patent ApplicationPublication No. 2004/0254602 A1, published Dec. 16, 2004, to Lehe atal., the contents of which are incorporated herein by reference.However, the concepts disclosed herein are equally applicable to singleended rapid exchange catheters.

Specifically, this invention applies to any catheter used in conjunctionwith a guidewire or elongate support member for delivery. The concept isuniversal. Embolic protection device delivery catheters, ballooncatheters, and stent delivery catheters with or without a balloon aretypical catheters to which the invention can be applied. The concept canalso be applied to percutaneous delivery and recovery catheters foratrial appendage occlusion devices, mitral valve remodeling devices,septal defect closure devices, and the like.

The components of the catheters of the invention are made frombiocompatible materials such as metals or polymeric materials. Ifnecessary, these metals or polymeric materials can be treated to impartbiocompatibility by various surface treatments, as known in the art.Suitable materials include stainless steel, titanium and its alloys,cobalt-chromium-nickel-molybdenum-iron alloy (commercially availableunder the trade designation ELGILOY™), carbon fiber and its composites,and polymers such as liquid crystal polymers, polyetheretherketone(PEEK), polyimide, polyester, high density polyethylene, PEBAX®, variousnylons, and the like. A shape memory or superelastic material such asnitinol or shape memory polymer is also suitable. The size, thickness,and composition of materials are selected far their ability to performas desired as well as their biocompatibility. It is to be understoodthat these design elements are known to one of skill in the art.

The material comprising the catheter is preferably at least partiallyradiopaque. This material can be made radiopaque by plating, or by usingcore wires, tracer wires, or fillers that have good X-ray absorptioncharacteristics compared to the human body. Marker bands comprised ofgenerally tubular radiopaque metals may be attached to the catheter.

The tip of the catheter may be a generally softer material so as to helpprevent damage to a vessel wall as the tip is advanced through thevasculature. Softer materials such as PEBAX®, nylon, rubbers, urethane,silicone, ethylene vinyl acetate, and the like may be attached to thecatheter by adhesives, overmolding, heat bonding, solvent bonding, andother techniques known in the art. The tip may have a geometry designedto assist with advancement of the catheter past intraluminalobstructions, such as any of those constructions contained within U.S.Pat. No. 6,979,343 B2, issued Dec. 27, 2005, to Russo et al., thecontents of which are incorporated by reference herein.

The catheter is generally referred to as an embolic protectiondelivery/recovery catheter however it is contemplated that theembodiments of the catheters described herein may be used solely fordelivery, solely for recovery, or for both delivery and recovery.

FIG. 1 shows a rapid exchange catheter 20 in accordance with the presentinvention. The catheter includes an elongated body 22 having first andsecond opposite end portions 24 and 26. The elongated body 22 ispreferably sufficiently flexible to allow the device to be advancedthrough a curving vascular pathway without kinking and withoutpuncturing the vessel wall. The first and second end portions 24 and 26are both capable of leading the elongated member 22 through thevasculature depending upon the direction the elongated member 22 isinserted into the vasculature. The first and second end portions 24 and26 are adapted for providing different functions. First end portion 24is adapted for deploying an indwelling medical device such as a stent,graft or embolic protection device while the second end portion 26 isadapted for retrieving an indwelling medical device such as a stem graftor embolic protection device. As stated previously the present inventionis directed to end portion 24 comprising the rapid exchange deliveryportion of the catheter. The concepts disclosed herein are equallyapplicable to single ended rapid exchange delivery catheters.Additionally, although certain dimensions are stated with respect to thedisclosed embodiments those dimensions are merely for purposes ofillustration and other dimensions, as known by those of skill in theart, are within the scope of the present invention.

Catheter 22 includes a wire reinforced midsection 28. This section maybe reinforced with a core wire 29 to enhance the pushability of thecatheter. The core wire may be 0.014 inch (0.036 cm) in diameter.

In the context of the present invention catheter 20 will be described interms of the use of the rapid exchange delivery catheter side.Therefore, unless otherwise stated, end portion 24 is referred to as thedistal end. End portion 24 includes distal port 25. The catheterincludes a distal portion 30 which may be approximately 15 centimetersin length. Distal portion 30 has a low crossing profile which is adaptedto allow that portion of the catheter to cross a lesion in thevasculature. For example, distal portion 30 may have an outer diameterof approximately 0.042 inch (0.11 cm). Just proximal of distal portion30 is a housing portion 32. Housing portion 32 has a slightly increasedID and OD as compared to distal portion 30 for the purpose of providinga housing section for a medical device such as an embolic protectiondevice which will be described in more detail hereafter. Elongate member22 includes an exit port 34 which is spaced proximally of housingsection 32. For example, exit port 34 may be spaced 5 centimeters fromhousing portion 32 and 30 centimeters from end portion 24. Exit port 34is sized to allow passage of both a primary guidewire and a host wirethat carries an embolic protection device. Elongate member 22 includes asecond exit port 36 for use in connection with the recovery side ofcatheter 20. Housing portion 32 may be at least semitransparent toensure appropriate loading of the embolic protection device or othermedical device both during packaging and even during use of the deviceby a physician.

FIG. 2 is another view of catheter 20 showing housing portion 32, aportion of distal portion 30 and exit port 34. In this figure theprimary guidewire 38 has been loaded into the lumen of catheter 20 andexits through exit port 34. Within housing section 32 is a housingmember 40 into which has been loaded an embolic protection device 42carried by a support wire or host wire 44. Housing member 40 is shown ascomprising a tubular shaped structure. However, other shapes arecontemplated within the scope of the invention. Housing member 40defines an interior cavity or space for containing the embolicprotection device in its collapsed or delivery configuration. Theexterior dimensions of housing member 40 are selected such thatsufficient space is left within housing section 32 to allow for passageof the primary guidewire. Host wire 44 also exits the catheter lumenthrough exit port 34. Housing member 40 can be secured at a fixedlocation within housing section 32 as described in connection with FIGS.5 to 7. Alternatively, housing member 40 may comprise a shuttlecomponent which can move axially within housing section 32 betweendistal and proximal ends of the housing section as described inconnection with FIGS. 3 and 4.

FIG. 3A discloses an embodiment wherein housing member 40 is configuredto move axially within housing section 32 between a reduced diameter end46 of housing section 32 and a stop member 48 which is attached orbonded within the lumen of catheter 20 at the proximal end of housingsection 32. Stop member 48 is provided with one or more openings orslots 50 and 52. Stop member 48 is shown in more detail in FIG. 4. Thestop member is sized and configured to ensure that housing member 40will not wedge into the proximal transition between the larger diameterhousing section 32 and the adjacent smaller diameter proximal portion ofthe catheter. If the housing member were to wedge into this proximaltransition section the primary guidewire would be prevented from passingaround the shuttle thereby blocking its access to the proximal sectionof the catheter and exit port 34. Stop member 48 functions to spacehousing member 40 distally of the proximal end of housing section 32.Slots 50 and 52 are sized to ensure that the primary guidewire is ableto pass through the slots into the proximal section of the catheter toaccess the exit port. FIG. 3B shows the embodiment of FIG. 3A where boththe primary guidewire 38 and the embolic protection device 42 have beenloaded into the delivery catheter. The primary guidewire 38 passesthrough the exit port 34 and distal port 25.

FIGS. 5A, 5B and 5C disclose alternative embodiments of the catheterwhere housing member 40 is secured at a fixed location within housingsection 32. Each of these embodiments incorporates a mechanism to freezethe housing member or shuttle within housing section 32. The mechanismmay be in the form of a support structure that will suspend the housingor shuttle inside of the housing section. This prevents movement of thehousing within the catheter hut will still allow loading of the embolicprotection device, passage of the primary guidewire around the shuttleinto the proximal end of the catheter and out the exit port. Themechanism for suspension of the housing is designed to allow adequateclearance both distally and proximally to ensure space for the primaryguidewire to pass. The suspension structure is also configured to lowthe wire to pass around the housing. The suspension mechanism may retainthe housing to one side of the catheter lumen. The suspension mechanismmay be, for example, a clasp, rib-like structure, washer-like structure,or other material embedded into the wall of the catheter lumen. Thesuspension piece can be constructed of the catheter material itself orcan be an independent piece either wedged or adhered to the catheterinner wall.

In the embodiment shown in FIG. 5A a housing member 40 a has a proximalportion 54 winch is affixed or bonded to the inner wall of catheter 20at the proximal end of housing section 32. Housing member 40 a isprovided with one or more slots 56 and 58 which are sized to allowpassage of the primary guidewire from the distal end of the catheter outexit port 34 (not shown). Housing member 40 a is sized to allowsufficient space between housing member 40 a and the inner wall ofhousing section 32 so that the primary guidewire can be passed. FIG. 6Ais a cross-sectional view of housing member 40 a disclosed in FIG. 5A.FIG. 6B is a cross-sectional view of an alternative configuration ofhousing member 40 a which includes a reduced diameter section 60 whichcreates a step which acts as a stop when positioning the embolicprotection device within housing member 40 a.

In the embodiments of FIGS. 5B and 5C the housing member is suspendedwithin housing section 32 by use of a grommet which is sized to have anouter periphery which can be affixed to the inner wall of the catheterin the housing section. In FIG. 58 a grommet 62 comprises a multi-lumenextrusion which can be heat bonded to the catheter lumen. As shown inFIG. 7B grommet 62 comprises an opening 64 to receive housing member 40b and one or more openings 66 and 68 that allow passage of the primaryguidewire.

In the embodiment of FIG. 5C a dual lumen extruded grommet 70 isprovided. As shown in FIG. 7A grommet 70 comprises a dual lumenextrusion having a first opening 72 to receive housing member 40 c and asecond opening 74 to allow passage of the primary guidewire. In thisembodiment housing member 400 is positioned to one side of the housingsection 32 allowing adequate clearance for passage of the primaryguidewire. In this embodiment housing member 40 c includes a reduceddiameter portion to act as a stop for the embolic protection device. Thegrommets could alternatively be fabricated with metal or rubbercomponents.

FIGS. 8A to 8F show in simplified form the steps of loading and usingthe rapid exchange delivery catheter of the present invention. Thesesteps are generally applicable to all of the embodiments disclosedherein including those embodiments where the housing member isconfigured to move or float within the housing section and thoseembodiments where the housing member is suspended or fixed at aparticular location within the housing section.

FIG. 8A shows a distal portion of the catheter prior to loading ofeither an embolic protection device or the primary guidewire. In FIG. 8Bthe host wire 44 has been inserted through the lumen of the catheter,through housing member 40 and out exit port 34. This depicts a partiallypreloaded configuration of the embolic protection device within thecatheter. The catheter and embolic protection device may be packagedwithin this partially preloaded configuration. In FIG. 8C the embolicprotection device has been withdrawn proximally so that it is containedwithin housing member 40. In FIG. 8D the catheter and filter have beenloaded over the primary guidewire 38. The distal end of the guidewire ishack loaded through the distal end of the catheter. Since the embolicprotection device takes up the entire lumen of housing member 40 theguidewire is directed around housing member 40 as the catheter is movedover the guidewire. The lumen of the proximal delivery portion of thecatheter may end at exit port 34. The catheter may be provided with anoptional ramp 35 or other structure which causes the distal end of theguidewire to be directed out exit port 34 as the catheter is moved overthe guidewire.

Once the guidewire has been loaded over the guidewire it may be advancedthrough the vasculature to a treatment location as shown in FIG. 8E. Thetreatment location may comprise a lesion 76 which is crossed by thedistal portion 30 of the catheter. In FIG. 8E the primary guidewire hasbeen removed. The filter is deployed out of the distal end of thecatheter by urging the host wire distally. Once the embolic protectiondevice is deployed the delivery catheter is removed. The host wire canthen be used as a guidewire for an interventional treatment device ofchoice such as a balloon catheter and/or a stent delivery catheter. InFIG. 8F an embolic protection device in the form of a filter is showndeployed at a location distal to lesion 76. A stent 78 has been deployedat the lesion. The recovery end of the catheter 20 is shown advancedover the host wire 44. The recovery end of the catheter preferably has ashapeable tip which can be angled or bent to facilitate tracking therecovery catheter through the deployed stent. The shapeable tip may bemade of any of the materials that are described herein as being suitablecomponents of the catheters. In particular, the shapeable tip may beheat-treated to be made more ductile, and may be made of a shape memoryor super elastic alloy. Once the distal end of the recovery catheter haspassed through the stent the embolic protection device can be withdrawnproximally into the lumen of the recovery catheter. The embolicprotection device and recovery catheter are then withdrawn together fromthe vessel.

FIGS. 9A and 9B show additional features or configurations of theinvention. FIG. 9A shows an alternative distal tip which can beincorporated into the design of host wire 44. Host wire 44 may include aconfiguration which tapers in a stepped manner from a diameter of 0.014inch (0.036 cm) to 0.010 inch (0.025 cm) and then finally to 0.006 inch(0.015 cm). This stepped taper feature allows for more support andpushability of host wire 44 during delivery of the embolic protectiondevice. As shown in FIG. 9A, the transition region from a diameter of0.014 inch (0.036 cm) to 0.010 inch (0.025 cm) may have a length of 2.0inches (5.1 cm). The 0.010 inch (0.025 cm) diameter region may have alength of 2.35 inches (5.97 cm). The transition region from a diameterof 0.010 inch (0.025 cm) to 0.006 inch (0.015 cm) may have a length of0.25 inch (0.64 cm).

FIG. 9B shows a delivery tip transition component which can be used atthe distal tip of the delivery catheter. Delivery tip transitioncomponent 80 is an optional component which may be used for the purposeof reducing the opening at the distal tip of the delivery catheter to asize which is more compatible with the size of the primary guidewire.For example, the primary guidewire may have a diameter of 0.014 inch(0.036 cm). Thus, in the embodiment disclosed in FIG. 9B the transitioncomponent 80 has a distal opening of 0.016 inch (0.041 cm). This allowsthe catheter to track over the guidewire with a tighter fit providingmore fed fix the user. Transition component 80 may comprise a tearablespirally wrapped material which includes a string 82 which extendsoutside of the patient along side the delivery catheter. Once thedelivery catheter is positioned the transition component can be removedby pulling string 82 in a proximal direction. This provides additionalclearance for deployment of the embolic protection device from thedistal end of the delivery catheter.

Another feature of the device is shown in FIGS. 10A and 10B.Specifically, the catheter may be packaged with a removable packagingsheath 84. Packaging sheath 84 has an end that is adapted to accommodatea fluid filled syringe (not shown). The syringe may be used to flush theembolic protection device 42 and catheter 20 when they are prepared foruse. FIGS. 10A and 10B show fluid being flushed from the distal end tothe proximal end of the delivery catheter 20.

B. Embolic Filter with Centered Wire

The invention encompasses the use of any filtration device to bedeployed in a lumen or vessel of a patient. Although the examples relategenerally to filter protection devices deployed distal to a treatmentsite, the device can also be deployed proximal to a treatment site inconnection with interrupting or reversing flow through the vessel. Inthe case of a proximally deployed device, it will be advantageous toconstruct the device on a hollow elongate member so as to preserveaccess to the treatment site through the hollow member.

In a preferred embodiment, the distal protection system comprises acatheter that is loaded with an elongate support member or guidewireabout which is disposed a distal protection filter. The elongate supportmember is structurally similar to a traditional guidewire in somerespects. However, it is not used as a means at navigating the patient'svascular system and, therefore, does not need to be provided with all ofthe features of flexibility and steerability as does a traditionalguidewire. With these differences in mind, the terms elongate supportmember and guidewire may be used interchangeably herein. A floppy tip(described further below) may be at the distal end of the elongatesupport member or guidewire. Typically, the filter is introduced into ablood vessel through an introducing catheter.

Methods of introducing guidewires and catheters and the methods for theremoval of such devices from vessels are well known in the art ofendovascular procedures. In a typical procedure using the device of thisinvention, the elongate support member and filter are loaded into anintroducing sheath or catheter and moved into the vessel and through thecatheter to the treatment site. Typically, this is done by advancing afirst, or introduction guidewire, through the vessel to the region ofinterest. A catheter is advanced over the guidewire to the region ofinterest, and the guidewire removed. Then the filter or other functionaldevice carried by the elongate support member is advanced down acatheter sheath to the region of interest but within the catheter. Thecatheter sheath is withdrawn to deploy (expand) the filter at the regionof interest. Alternatively, the filter is preloaded into a catheter andheld in place by an outer sheath of the catheter and they are togetheradvanced through the vessel to the region of interest without using aninitial guidewire. In this embodiment the catheter/filter combinationwill be used to navigate through the vessel to the region of interest.Then the catheter is withdrawn to deploy the filter.

Typical dimensions of a filter used in the devices of this inventionrange from 2 nm to 90 mm in length, and from about 0.5 mm to 2 mm indiameter before deployment, and from about 2 mm to 30 mm in diameterafter deployment. A typical guidewire is about 0.2 to 1.0 mm in diameterand ranges from 50 cm to 320 cm in length.

The components of the distal protection system are made frombiocompatible materials. Materials also may be surface treated toproduce biocompatibility. The elongate support member may be formed ofany material of suitable dimension, and preferably comprises metal wire.Suitable materials include stainless steel, titanium and its alloys,cobalt-chromium-nickel-molybdenum-iron alloy (commercially availableunder the trade designation Elgiloy™), carbon fiber and its composites,and engineered polymers such as liquid crystal polymers,polyetheretherketone (PEEK), polyimide, polyester, and the like. A shapememory or superelastic metal such as nitinol is also suitable. Theelongate support member may be solid or may be hollow over some or allof its length.

The material used to make the filter or filter support structure ispreferably self-expanding. Suitable materials include metals such asstainless steel, titanium and its alloys, cobalt-chromium-nickelmolybdenum-iron alloy (commercially available under the tradedesignation Elgiloy™), carbon fiber and its composites, and engineeredpolymers such as liquid crystal polymers, polyetheretherketone (PEEK),polyimide, polyester, silk, and the like. A shape memory or superelasticmetal is particularly suitable for those applications when it is desiredfor an element, such as a filter, to assume a pre-determinedthree-dimensional shape or for a guidewire to maintain a pre-determinedcurvature. A shape memory or superelastic metal comprising nickel andtitanium known as “nitinol” is commercially available in variousdimensions and is suitable for use as both a guidewire and a filter. Forexample, nitinol tubular braid can be heat set into a desired shape,compressed for delivery to a site, and then released to resume theheat-set shape.

The filter element has a body defining an interior cavity. The filterbody has a plurality of openings or pores such that, when the filterelement is in its deployed configuration within the vessel lumen, fluidflows through the filter element and particles of the desired size arecaptured inside the interior cavity of the filter element.

The filter may comprise any material that is suitably flexible andresilient, such as a mesh, a material having openings or pores. Thefilter may comprise braided, knitted, woven, or non-woven fabrics thatare capable of filtering particles, preferably having pore sizes from 30to 500 microns. Woven or non-woven fabrics may additionally be treatedto fuse some or all of the fiber intersections. The fabric may be spunor electrospun. Suitable materials include those formed from sheets,films, or sponges, polymeric or metallic, with holes formed bymechanical means such as laser drilling and punching, or by chemicalmeans such as selective dissolution of one or more components. Forexample, a suitable filter material is braided tubular fabric comprisingsuperelastic nitinol metal. Mesh fabric of nitinol material can beheat-set to a desired shape in its expanded configuration.

The material comprising the filter is preferably at least partiallyradiopaque. This material can be made radiopaque by plating, or by usingcore wires, tracer wires, or fillers that have good X-ray absorptioncharacteristics compared to the human body. Radiopaque filters aredescribed in U.S. Patent Application Publication No. 2002/0188314 A1,published Dec. 12, 2002, to Anderson et al., the contents of which arehereby incorporated by reference herein.

The embodiments of this invention, described in detail below inconnection with the figures, are suitable for use with various distalprotection systems that are known in the art. The filter may have awindsock type shape. The construction, deployment and retrieval of afilter having this shape is described, for example, in U.S. Pat. No.6,325,815 B1, issued Dec. 4, 2001, to Kusleika et al., the contents ofwhich are hereby incorporated by reference herein. Other features offilters relevant to the invention disclosed herein are described in U.S.Pat. No. 6,773,448 B2, issued Aug. 10, 2004, to Kusleika et al., U.S.Patent Application Publication No. 2003/0171771 A1, published Sep. 11,2003, to Anderson et al., and U.S. Patent Application Publication No.2004/0153119 A1, published Aug. 5, 2004, to Kusleika et al., thecontents of each of which are incorporated herein by reference.

The filter may also be a cup-shaped or basket-shaped device that mayform a proximally facing opening when expanded. The construction,deployment, and retrieval of such a filter is described in WO 96/01591(Mazzocchi et al.). This cup-shaped device may generally resemble anumbrella or a parachute, having a dome-like structure curving radiallyoutwardly from the guidewire or elongate support member. Other shapesmay be equally suitable in performing a filtering function, such as aconical shape, or a relatively flat disc shape. It will be appreciatedthat the shape of these filtration devices shown in various embodimentsare merely illustrative and are not meant to limit the scope of theinvention.

Regardless of the shape of the filter, the filter preferably is deployedusing an elongate support member. This can be done in various ways, andone or both of the proximal and distal ends of the filter may be affixedto the elongate support member (by a fixed element) or may be slidablydisposed about the elongate support member (by one or more slidingelements).

One type of sliding element comprises inner and outer annular rings. Thefirst ring fits within the second ring. The inner diameter of the firstring is larger than the diameter of the elongate support member so thatthe sliding element can slide over the elongate support member. Thesliding element can be affixed to the filter fabric by placing thefabric between the first and second rings. However, this is not meant tobe limiting, and the filter fabric can also be affixed to the slidingelement by adhesive, solder, crimping, or other means known in the art.The sliding element may comprise any stiff material such as metal orpolymer and preferably the slider is radiopaque. Suitable materialsinclude stainless steel, titanium, platinum, platinum/iridium alloy,gold alloy, polyimide, polyester, polyetheretherketone (PEEK), and thelike. Movement of a sliding element with respect to the elongate supportmember can be facilitated by coating one or both of the inside of thesliding element and the outside of the elongate support member with afriction-reducing coating, such as polytetrafluoroethylene or alubricious hydrophilic coating.

Fixed elements include annular rings. Also included within this meaningis an element that is crimped, adhered, soldered, or otherwise fasteneddirectly to the elongate support member. Also, the filter fabric may beattached directly to the elongate support member. In any event, thesliding and fixed elements (or any attachment point) typically compriseradiopaque material to assist in the placement of the filter. Inaddition, one or more radiopaque markers may be positioned at variouslocations on the protection device. These radiopaque markers or marketbands comprise a material that will be visible to X-rays and they assistin positioning the device.

Some distal protection filters include a floppy tip at a distal portionof the guidewire or elongate support element. The floppy tip provides anatraumatic and radiopaque terminus for the device. An atraumatic tipprevents vessel injury during initial placement or subsequentadvancement of the device. A radiopaque tip helps the physician verifysuitable tip placement during fluoroscopy. The floppy tip preferablycomprises a springy or resilient material, such as a metal (e.g.,stainless steel, iron alloys such as Elgiloy™, platinum, gold, tungsten,and shape memory or superelastic metal such as nitinol) or polymer(e.g., polyetheretherketone (PEEK), polyimide, polyester,polytetrafluoroethylene (PTFE), and the like). Springy materials aredesirable because they tend to retain their shape. The physician willinitially shape the tip, typically with a slight curve, and then as thedevice is advanced through the body the tip will be deflected as itencounters obstacles. It is desirable, after the inevitable deflectionsduring insertion, that the tip restores itself to the pre-set shape.Polymeric materials additionally may be reinforced with metals or otherfillers. The tip may be a monofilament or multifilament (such as acable). The floppy tip may be tapered or have a uniform diameter overits length. The floppy tip may comprise a tube, or could have circular,flat, or other cross-sections. It may be coiled. The tip may compriseone or more elements (for example, parallel independent structures). Thetip may be polymer-coated or otherwise treated to make the surfaceslippery. The floppy tip can be any desired length.

The filter comprises biocompatible materials such as metals andpolymeric materials. Materials such as metals and polymeric materialscan be treated to impart biocompatibility by various surface treatments,as known in the art. When wire is used, the wire is selected on thebasis of the characteristic desired, i.e., stiffness or flexibility, andthe properties can depend upon both the diameter of the wire and itscross-sectional shape. The size, thickness, and composition of elasticmaterials are selected for their ability to perform as desired as wellas their biocompatibility. It is to be understood that these designelements are known to one of skill in the art.

The present invention includes a host wire for an embolic filter devicethat has a side branch or rail for the filter to be positioned in such amanner that the host wire portion of the device remains centered in thevessel in which the filter is deployed. Various embodiments of theinvention are disclosed which include the provision for some type ofside branch or rail positioned at or near the distal end of the hostwire. This side branch or rail may be created by splitting the distalend of the wire in half or by attaching an additional wire to the mainhost wire. The wire branch that has been created by this design anglesaway from the main host wire. A portion of the embolic filter isretained on this side branch resulting in the positioning of the filterto one side of the vessel wall. The angle of the side branch allows themain wire to remain centered in the vessel. This side branch mayreattach to the main wire at a more distal location from the main angleseparation point. Typically, the filter is configured to move freelylongitudinally along this side branch. In addition the side branch mayrotate axially around the main wire to allow rotational movement of themain wire without affecting the filter position in the vessel. Thus, thedesign allows both rotational and longitudinal movement of the host wirewithout disruption of the position of the deployed filter device withinthe vessel. This is accomplished by providing in the various embodimentsa combination of rotateable, sliding elements and stops. This conceptprovides for excellent device wall apposition with minimized wire biasand filter movement and maximizes the filtration capabilities of thefilter within the vessel.

The unproved embolic filter device disclosed herein is used in a mannerconsistent with embolic filtration devices such as the embolic filterdevice 90 disclosed in FIG. 11. A potential disadvantage of this filteris that, under certain circumstances, the proximally facing mouth of thefilter may not fully open when the filter is deployed. This is becausethe circumference of the filter mouth is attached to the support wire.Thus, if the support wire is spaced from the vessel wall where thefilter is deployed the mouth of the filter may not fully open. Thepresent invention overcomes that problem.

The filter may be preloaded onto the delivery end of the catheterdescribed previously and advanced to the treatment location over theprimary guidewire. The guidewire is then removed and filter and hostwire advanced and deployed from the distal end of be delivery catheter.The delivery catheter is removed, the primary intervention is performedover the device host wire (for example angioplasty or, stenting) andupon completion of the primary intervention, the recovery catheter endof the previous device is advanced to recover the filter and host wirefor removal as described previously. Other delivery catheters, recoverycatheters and combined delivery/recovery catheters can also be used.

The improved embolic filter device embodiments disclosed herein act tocenter the wire within the vessel where the filter is deployed. Thisprevents wire bias that can cause the filter mouth to collapse or havereduced wall apposition. The design provides minimal obstruction to theentrance of the filter device while allowing the host wire to remaincentered in the vessel. Various embodiments of the improved embolicfilter device are disclosed in FIGS. 12 to 17.

FIG. 12 discloses an embolic filter device 100 a carried on a host wire102. Host wire 102 includes a side branch 104, Side branch 104 isrotateably and slideably attached at its ends by sliders 104 a and 104b. Embolic filter device 100 a has a proximal slider 106 and a distalslider 108. Proximal slider 106 is adapted to slide over side branch 104while distal slider 108 is adapted to slide over host wire 102.Longitudinal movement of the embolic filter and side branch 104 islimited both proximally and distally by stops 109 a and 109 b.

FIG. 13 discloses an embolic filter device 100 b which is carried by ahost wire 112. Host wire 112 includes a forked portion 114 having adistal stop 114 a. Forked portion 114 is connected rotateably andslideably to host wire 112 by slider 114 b. Embolic filter device 100 bhas a proximal slider 116 and a distal slider 118. Proximal slider 116is configured to slide along fork 114 between its connection point at aproximal end to host wire 112 and distal stop 114 a. Distal slider 118is configured to slide over host wire 112. Longitudinal movement of theembolic filter and forked portion is limited both proximally anddistally by stops 119 a and 119 b.

FIG. 14 discloses an embolic filter device 100 c carried by a host wire122. Host wire 122 is provided with a looped portion 124. Embolic filterdevice 100 c has a proximal slider 126 and a distal band 128. Proximalslider 126 of embolic filter device 100 c is configured to slide overthat portion of the looped portion 124 that is spaced apart from hostwire 122. In this embodiment rotation of the host wire 122 cannot bedone without affecting the position of filter device 100 c.

FIG. 15 snows embolic fitter device 100 d carried by a host wire 132.Host wire 132 has an enlarged distal end 132 a that is indeliblyreceived in a tube 135. Host wire 132 has a branch 134. One end ofbranch 134 is rotateably and slideably connected to host wire 132 atslider 134 a. Embolic protection device 100 d has a proximal slider 136adapted to slide over branch 134 and a distal slider 138 which slidesover an extending portion of branch 134. Branch 134 is fixed between itsproximal and distal ends to tube 135.

FIG. 16 discloses an embolic filter device 100 e carried by host wire142. Host wire 142 has a slot 144 adapted to receive a sliding element146. Sliding element 146 is connected by wire 148 to a proximal end 150of embolic filter device 100 e. Wire 148 is sized and shaped to centerhost wire 142 in the proximal opening of embolic filter device 100 ewhen deployed in a lumen. Embolic filter device 100 e includes distalslider 152 which is configured to slide over a distal portion of hostwire 142. Host wire 142 is provided with some range of axial movementwith respect to embolic filter device 100 e by virtue of sliding element146 and distal slider 152.

FIG. 17 discloses an embolic filter device 100 f carried by host wire154. Host wire 154 has a tapered portion 156 bounded at a distal end bystop 158. Embolic filter device 100 f includes a proximal end 161 whichis connected to slider 160 by wire 163. Slider 160 slides over host wire154 over a range of motion bounded by tapered portion 156 and distalslider 162 slides over a distal portion of host wire 154.

The foregoing detailed description should be read with reference to thedrawings and which like elements in different drawings are numberedidentically. The drawings, which are not necessarily to scale, depictselected embodiments and are not intended to limit the scope of theinvention. Several forms of invention have been shown and described, andother forms will now be apparent to those skilled in the art. It will beunderstood that embodiments shown in drawings and described above aremerely for illustrative purposes, and are not intended to limit thescope of the invention as defined in the claims which follow.

What is claimed is:
 1. A system comprising: a guidewire; a cathetercomprising: an elongated member configured to be advanced along avascular path of a patient, the elongated member comprising a proximalportion, a distal portion, a proximal end, a distal end, a housingportion adjacent to and proximal of the distal portion, and a sidewallexit port proximal of the housing portion, the sidewall exit port beingdimensioned to receive the guidewire, the distal end comprising a distalport, the housing portion defining an interior cavity; and a housingmember contained within the interior cavity, the housing member havingan interior space dimensioned for housing an indwelling medical device,and the housing member having a proximal end that is distal of theproximal end of the elongated member, and the elongated membercomprising a lumen extending at least from the exit port to the distalport, the housing member being disposed within the lumen and the lumenencompassing the interior cavity of the housing portion, wherein theguidewire is configured to extend through the distal port, through aportion of the lumen in the housing portion, the portion extendingbetween an interior surface of the housing portion and an exteriorsurface of the housing member, and through the exit port.
 2. The systemof claim 1, wherein the housing member is secured at a fixed locationwithin the housing portion.
 3. The system of claim 1, wherein thehousing member is configured to move axially within the housing portion.4. The system of claim 3, wherein the housing portion comprises distaland proximal housing sections, and wherein the housing member isconfigured to move axially between the proximal and distal sections ofthe housing portion.
 5. The system of claim 4, wherein the proximalhousing section comprises a stop member.
 6. The system of claim 5,wherein the stop member defines one or more sidewall slots configured todefine pathways for the guidewire.
 7. The system of claim 1, wherein thehousing portion and the distal portion have outer diameters and theouter diameter of the housing portion is larger than the outer diameterof the distal portion.
 8. The system of claim 1, wherein the housingportion and the distal portion have inner diameters and the innerdiameter of the housing portion is larger than the inner diameter of thedistal portion.
 9. The system of claim 5, wherein the housing portionand the distal portion have inner diameters and the inner diameter ofthe housing portion is larger than the inner diameter of the distalportion.
 10. The system of claim 1, wherein the elongated membercomprises an inner wall defining the lumen and the housing member isadjacent to the inner wall.
 11. The system of claim 1, wherein thehousing member is centered within the lumen.
 12. The system of claim 1,wherein the housing member is tubular.
 13. The system of claim 1,further comprising a ramp in the lumen configured to direct theguidewire out the exit port when the guidewire is in the lumen.
 14. Thesystem of claim 1, wherein the proximal portion comprises an indwellingmedical device retrieval structure.
 15. The system of claim 1, whereinat least a portion of the housing portion is transparent.
 16. The systemof claim 1, wherein the proximal end of the elongated member comprises arolled tip.
 17. The system of claim 1, wherein the proximal end of theelongated member comprises a shapeable tip.
 18. An assembly comprising amedical device and the system of claim 1, wherein the medical device isconfigured to be delivered and retrieved by the elongated member. 19.The assembly of claim 18, wherein the medical device comprises anembolic protection device, a balloon catheter, a stent deliverycatheter, an atrial appendage occlusion device, a mitral valveremodeling device, or a septal defect closure device.
 20. The assemblyof claim 18, wherein the medical device is an embolic protection device.21. The assembly of claim 20, wherein the embolic protection device is afilter.
 22. The assembly of claim 20, wherein the embolic protectiondevice is an occlusive device.
 23. An assembly comprising the system ofclaim 1 and a removable packaging sheath having an end adapted toaccommodate a fluid filled syringe for flushing the elongated member.24. A method for positioning a medical device within a patient's bloodvessel, the method comprising: placing the medical device within ahousing member contained within an interior cavity of a catheter, thecatheter comprising: an elongated member configured to be advanced alonga vascular path of a patient, the elongated member comprising a proximalportion, a distal portion, a proximal end, a distal end, a housingportion adjacent to and proximal of the distal portion, and a sidewallexit port proximal of the housing portion, the sidewall exit port beingdimensioned to receive the guidewire, the distal end comprising a distalport, the housing portion defining the interior cavity, the elongatedmember comprising a lumen extending at least from the exit port to thedistal port, the housing member being disposed within the lumen and thelumen encompassing the interior cavity of the housing portion, thehousing member having a proximal end that is distal of the proximal endof the elongated member; advancing the catheter to a target site withinthe patient's blood vessel over a guidewire, the guidewire extendingthrough the distal port, through a portion of the lumen in the housingportion, the portion extending between an interior surface of thehousing portion and an exterior surface of the housing member, andthrough the exit port; and advancing the medical device out of thecatheter to the target site within the patient's blood vessel.
 25. Amethod for positioning a catheter within a patient's blood vessel, themethod comprising: advancing a guidewire to a target site within thepatient's blood vessel; and advancing a catheter over the guidewire, thecatheter comprising: an elongated member configured to be advanced alonga vascular path of a patient, the elongated member comprising a proximalportion, a distal portion, a proximal end, a distal end, a housingportion adjacent to and proximal of the distal portion, and a sidewallexit port proximal of the housing portion, the sidewall exit port beingdimensioned to receive the guidewire, the distal end comprising a distalport, the housing portion defining the interior cavity, the elongatedmember comprising a lumen extending at least from the exit port to thedistal port, a housing member being disposed within the lumen and thelumen encompassing the interior cavity of the housing portion, thehousing member having a proximal end that is distal of the proximal endof the elongated member, wherein advancing the catheter over theguidewire comprises inserting the guidewire through the lumen betweenthe distal port and the sidewall exit port, such that the guidewireextends through the distal port, through a portion of the lumen in thehousing portion, the portion extending between an interior surface ofthe housing portion and an exterior surface of the housing member, andthrough the exit port.
 26. The method of claim 25, wherein an embolicprotection device is loaded into the catheter prior to advancing thecatheter over the guidewire.
 27. The method of claim 26, wherein thecatheter is advanced over the guidewire to a treatment site, theguidewire is removed, and the embolic protection device is advanced outof the catheter.